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  2. Zep (company) - Wikipedia

    en.wikipedia.org/wiki/Zep_(company)

    Zep was founded in 1937 by Mandle Zaban, William Eplan, and Saul Powell. [2] The company manufactured industrial and janitorial cleaning products and differentiated itself from competitors through marketing its product formulations as unique and promoting their hands-on customer service. [3]

  3. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  4. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Linear alkylbenzenes (sometimes also known as LABs) are a family of organic compounds with the formula C 6 H 5 C n H 2n+1. Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12-C 15, C 12-C 13 and C 10-C 13, for detergent use. [1] The C n H 2n+1 chain is unbranched.

  5. 4-Methylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Methylbenzaldehyde

    4-Methylbenzaldehyde is the aromatic aldehyde with the formula CH 3 C 6 H 4 CHO. It is a colorless liquid. It is a colorless liquid. Commercially available, it may be prepared from the Friedel-Crafts formylation of toluene with carbon monoxide and hydrogen chloride under Gattermann-Koch conditions .

  6. Bis(2-ethylhexyl) phthalate - Wikipedia

    en.wikipedia.org/wiki/Bis(2-ethylhexyl)_phthalate

    Bis(2-ethylhexyl) phthalate (di-2-ethylhexyl phthalate, diethylhexyl phthalate, diisooctyl phthalate, DEHP; incorrectly — dioctyl phthalate, DIOP) is an organic compound with the formula C 6 H 4 (CO 2 C 8 H 17) 2. DEHP is the most common member of the class of phthalates, which are used as plasticizers.

  7. 3,5-Dinitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3,5-Dinitrobenzoic_acid

    3,5-Dinitrobenzoic acid finds use in the identification of various organic substances, especially alcohols, by derivatization.For such an analysis, the substance to be analyzed is reacted with 3,5-dinitrobenzoic acid in the presence of sulfuric acid in order to form a derivate.

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